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Seite 24 für „Gene“ · Literaturverweise aus öffentlichen Artikeln
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An unexpected cause of pancytopenia after allogeneic bone marrow transplant
pubmed · 41705798
Literaturverweis öffnenEndoGene database: reported genetic variants for 5,926 Russian patients diagnosed with endocrine disorders
pubmed · 40041282
Literaturverweis öffnenAcute Subglottic Laryngitis. Etiology, Epidemiology, Pathogenesis and Clinical Picture
pubmed · 31680234
Literaturverweis öffnenPathogenesis of sarcoidosis.
pubmed · 3310401
Literaturverweis öffnenRadiogenomics of congenital brain malformations: Linking embryology, genetics, and imaging
pubmed · 41670708
Literaturverweis öffnenX-chromosome gene dosage shapes MASLD beyond sex hormones
pubmed · 42191501
Literaturverweis öffnenNonsyndromic epidermal differentiation disorders: a new classification toward pathogenesis-based therapy
pubmed · 40308026
Literaturverweis öffnenOsteogenesis imperfecta
pubmed · 9088762
Literaturverweis öffnen[Androgenetic alopecia: finasteride treated hair loss].
pubmed · 10230220
Literaturverweis öffnenThick filament molecular interfaces play a critical role in the pathogenesis of hypertrophic cardiomyopathy
pubmed · 42372158
Literaturverweis öffnenThe favorable role of recombinant collagen peptide in periosteal cell-derived osteoregeneration
pubmed · 41567730
Literaturverweis öffnenA New Gene for Congenital Stationary Night Blindness
pubmed · 41343185
Literaturverweis öffnenVaginal Microecological Imbalance, Human Papillomavirus Infection, and Cervical Carcinogenesis: Mechanisms and Clinical Implications
pubmed · 42404294
Literaturverweis öffnenMolekulare Pathogenese von Schilddrüsenknoten – Bedeutung für die klinische Versorgung
pubmed · 28881369
Literaturverweis öffnenBilateral patellar tendon rupture following indirect trauma in a young patient due to suspected chronic tendon degeneration caused by repetitive microtrauma: A case report
pubmed · 42232473
Literaturverweis öffnenClinical and genetic spectrum of SHOX deficiency: phenotypic heterogeneity and the "Jumping SHOX" phenomenon
pubmed · 42230379
Literaturverweis öffnenA male infant with a novel heterogeneous nuclear ribonucleoprotein H1 variant, bilateral cataracts, dysplastic thumbs, and severe airway malacia
pubmed · 42204999
Literaturverweis öffnenSurgical Outcomes of Degenerative Cervical Myelopathy in Patients with Parkinson Disease: A Systematic Review
pubmed · 42427199
Literaturverweis öffnen[Detection and significance of BRAF gene in mature T/NK cell lymphoma]
pubmed · 26887510
Literaturverweis öffnen[Idiopathic epilepsy with generalized seizures in early childhood].
pubmed · 1435803
Literaturverweis öffnenFamilial Turner Syndrome With Distinct Karyotypes in Two Cousins: Phenotypic Convergence and Genotypic Heterogeneity
pubmed · 42108647
Literaturverweis öffnenIdentifying common genetic etiologies between iridocyclitis and related immune-mediated diseases
pubmed · 41624885
Literaturverweis öffnenDiagnostic heterogeneity in deltoid ligament repair studies: Implications for evidence synthesis
pubmed · 41967667
Literaturverweis öffnenA safer path to gene correction in junctional epidermolysis bullosa
pubmed · 41500227
Literaturverweis öffnenTargeted next-generation sequencing for drug-resistant tuberculosis diagnosis: implementation considerations for bacterial load, regimen selection and diagnostic algorithm placement
pubmed · 41192929
Literaturverweis öffnenCerebral palsy: causes, pathways, and the role of genetic variants
pubmed · 26003063
Literaturverweis öffnenWarfarin-Induced Developmental Toxicity: Insights into Embryogenesis, Teratogenicity, and Molecular Pathways
doi · 10.20944/preprints202606.1173.v1
Literaturverweis öffnenPhase separation and protein aggregation in neurodegenerative diseases
pubmed · 42418847
Literaturverweis öffnenEarly multimodal rehabilitation and functional outcomes of a left brachial plexus injury after general anesthesia: a case report
pubmed · 42317418
Literaturverweis öffnen[Wegener's granulomatosis and Wegener's Granuloma (author's transl)].
pubmed · 6109704
Literaturverweis öffnen